Clinical Research Coordinator - Impactful Trials

HC1316 GE Precision Healthcare LLC

New York (NY)

On-site

USD 55,000 - 75,000

Full time

4 days ago
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Job summary

HC1316 GE Precision Healthcare LLC is seeking a Clinical Research Coordinator to support cutting-edge research in healthcare. You will partner with study participants and teams, coordinate sessions, maintain regulatory compliance, and contribute to innovations that improve patient outcomes.

A strong focus on organization, communication, and attention to detail is essential. The role requires a hands-on approach with GCP/IRB knowledge and the ability to train and guide a large study staff, within

Qualifications

  • Bachelor's degree in science or a related field.
  • Minimum 2 years in clinical research.
  • Outstanding organizational skills.
  • Proficient in Microsoft Office (Excel, Outlook, Word).
  • Meticulous attention to detail.
  • Excellent communication skills (written and verbal).

Responsibilities

  • Recruit, screen, enroll, and obtain informed consent from study participants.
  • Coordinate study sessions, scheduling, space reservation, staff training, and documentation.
  • Ensure compliance with study protocol, regulations, GCP, IRB, and GE HealthCare processes.
  • Maintain study documentation including regulatory binders and trackers.
  • Complete IRB submissions and adverse event reports as required.
  • Provide guidance to study staff and prepare for audits.

Skills

Organizational skills
Communication skills
Attention to detail

Education

Bachelor's degree (science or related field)

Tools

Microsoft Office

Job description

HC1316 GE Precision Healthcare LLC is seeking a Clinical Research Coordinator to support cutting-edge research in healthcare. You will partner with study participants and teams, coordinate sessions, maintain regulatory compliance, and contribute to innovations that improve patient outcomes.

A strong focus on organization, communication, and attention to detail is essential. The role requires a hands-on approach with GCP/IRB knowledge and the ability to train and guide a large study staff, within

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